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Fire-resistant polymers containing bisphenol C and deoxybenzoin derivatives.

机译:含有双酚C和脱氧安息香衍生物的耐火聚合物。

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摘要

The synthesis, processing, and engineering of low heat release, ultra fire-resistant materials present an important challenge in polymer materials chemistry. One approach to this problem involves the use of materials that char upon decomposition rather than evolve flammable gas. Here, the synthesis and characterization of 1,1-dichloro-2,2-bis(4-hydroxyphenyl)ethene (bisphenol C or BPC) and deoxybenzoin containing polymers are described.;Poly(aryletherketone)s containing 1,1-dichloro-2,2-bis(4-hydroxyphenyl)ethene (BPC) were synthesized by the cesium fluoride initiated polymerization of 1,1-dichloro-2,2-bis(4-t-butyldimethylsiloxyphenyl)ethane with 4,4'-difluorobenzophenone (BP-F). These polymers exhibit high char yields by thermogravimetric analysis (TGA), and low heat release capacities were measured by pyrolysis combustion flow calorimetry (PCFC). Poly(aryletherketone)s were prepared from BP-F and various ratios of BPC and bisphenol-A (BPA), and their thermal properties were characterized by TGA and PCFC.;Fire-resistant bisphenol C and polydimethylsiloxane (PDMS) polyurethanes were prepared through the polycondensation of 1,1-dichloro-2,2-bis(4-isocyanatophenyl)-ethene (BPC-NCO) with BPC and 2000 g/mol hydroxybutyl-terminated PDMS (PDMS-BuOH). These polyurethanes showed increased char yields based on inclusion of BPC-NCO and PDMS-BuOH, and substantially reduced heat release capacities compared to similar polyurethanes prepared with 2,4-tolylene diisocyanate and poly(tetramethyleneoxide).;Halogen-free, fire-resistant copolyarylates were prepared by interfacial copolymerization of isophthaloyl chloride and several relative ratios of 4,4 '-bishydroxydeoxybenzoin and bisphenol A. The fire-resistance of these polyarylates was explored by TGA and PCFC, and char yields of nearly 40% were observed, twice that of bisphenol A polyarylate. Heat release capacities as low as 81 J/g·K were measured by PCFC. Thus, halogenation, often used to effect fire-resistance in materials, is eliminated all together.;Hyperbranched polyphenylenes with bromine and boronic acid termination were prepared by Suzuki coupling polymerization. An exceptionally low heat release capacity of 6 J/g·K were measured by PCFC for bromine terminated polymers and char yields were shown to increase as a function of boronic acid termination due to the formation of a glassy network.
机译:低热释放,超耐火材料的合成,加工和工程设计对聚合物材料化学提出了重要挑战。解决该问题的一种方法涉及使用在分解时会炭化而不是放出易燃气体的材料。本文描述了1,1-二氯-2,2-双(4-羟基苯基)乙烯(双酚C或BPC)和含脱氧安息香的聚合物的合成和表征。;含1,1-二氯-甲基的聚(芳基醚酮)通过1,1-二氯-2,2-双(4-叔丁基二甲基甲硅烷氧基苯基)乙烷与4,4'-二氟二苯甲酮的氟化铯引发的聚合反应合成2,2-双(4-羟苯基)乙烯(BPC)( BP-F)。这些聚合物通过热重分析(TGA)表现出较高的焦炭收率,并且通过热解燃烧流动量热法(PCFC)测量了较低的放热能力。用BP-F制备了聚芳醚酮,分别用不同比例的BPC和双酚A(BPA)进行了表征,并用TGA和PCFC对它们的热性能进行了表征。 1,1-二氯-2,2-双(4-异氰酸根合苯基)乙烯(BPC-NCO)与BPC和2000 g / mol羟丁基封端的PDMS(PDMS-BuOH)的缩聚反应。这些聚氨酯与BPC-NCO和PDMS-BuOH的结合表现出更高的炭收率,并且与由2,4-甲苯二异氰酸酯和聚四甲撑氧化物制得的类似聚氨酯相比,其排热能力大大降低。通过间苯二甲酰氯与4,4'-双羟基脱氧安息香素和双酚A的几种相对比例的界面共聚制备共聚芳基酸酯。通过TGA和PCFC探索了这些聚芳基酸酯的耐火性,观察到焦炭收率接近40%,是其的两倍。双酚A聚芳酯。通过PCFC测量的热释放能力低至81 J / g·K。因此,通常可以消除材料中耐火性的卤化现象就可以完全消除。通过PCFC对溴封端的聚合物测得的异常低的热释放能力为6 J / g·K,由于玻璃状网络的形成,焦炭收率随硼酸封端的增加而增加。

著录项

  • 作者

    Ellzey, Kenneth A.;

  • 作者单位

    University of Massachusetts Amherst.;

  • 授予单位 University of Massachusetts Amherst.;
  • 学科 Chemistry Polymer.
  • 学位 Ph.D.
  • 年度 2004
  • 页码 134 p.
  • 总页数 134
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 高分子化学(高聚物);
  • 关键词

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